Cabergoline - the latest in libido enhancement
Cabergoline increases the levels of dopamine
through its action of stimulating D2 receptor sites,
it is officially approved to assist in the treatment of Parkinson's disease,
as well as treat states of prolactinoma (i.e. prevent breast development
in men and reduce excess milk secretion in women).
However, cabergoline (brand name Dostinex has been described as
being able to do everything that Viagra can’t! This is because rather
than induce an erection (as Viagra can); cabergoline has been shown to
improve libido, orgasm and ejaculation (which Viagra has not).
Cabergoline is from the dopaminergic family of drugs that increase the
level of dopamine and also decreases the levels of the hormone
prolactin. Prolactin is the hormone secreted in women after giving birth
and to enhance their lactation for breast feeding. However, prolactin
has recently been shown to be an inhibitor to a healthy libido, this may
help explain why many women have a low sex drive after giving birth-
whilst they are breast feeding. But men can also suffer from
prolactinoma (high levels of prolactin) leading to a lack of sex drive- as
well as developing breasts, particularly as prolactin levels tend to
increase for most men with age.
Recently it has been discovered that prolactin is released immediately
after an ejaculation and may be part of the reason men like to go sleep
after sex with no will for further love making.
Cabergoline has been proven to significantly decrease prolactin and in
so doing increase the sex drive (libido) substantially. There have been
reports of enhanced and multiple orgasms as well as stronger
ejaculations.
To date, bromocriptine has been the main drug of choice to reduce
prolactin levels, however clinical studies have confirmed that
cabergoline is much more effective in this regard. For example in 450
tested subjects over 8-weeks 77% of the subjects had their prolactin
levels returned to normal using 0.5mg of cabergoline twice a week,
compared to 59% of subjects using bromocriptine at 2.5mg twice a day.
Furthermore, side effects were far fewer in the cabergoline group,
recorded at 2% of incidences compared with 60% of those taking
broinocriptine.
One fascinating trial on 60 healthy males, between the ages of 22 and
31 discovered that they needed a break of 19 minutes between love
making. However, after taking cabergoline, they were able to have
several orgasms within a few minutes!
Dr. Schedlowski went on to say; "We interviewed the subjects and
found they were able to have multiple orgasms in very rapid
succession. This is sitting very nicely with our hypothesis that orgasms
and sexual drive are steered by prolactin and dopamine in the brain."
Furthermore, cabergoline had no side effects on men during the tests;
this was reported in an article for the International Journal of Impotence
Research. The researchers now plan to carry out trials to investigate
whether cabergoline will have the same effect on women.
Another medical study by the Federico University, in Naples, Italy
published in the European Journal of Endocrinology showed
cabergoline to be very potent in increasing libido and sexual potency.
The study examined cabergoline vs. bromocriptine (Par~odelâ) and
proved that cabergoline was superior in all respects to bromocriptine.
17 males with prolactinoma were treated with cabergoline or
bromocriptine for 6 months. All patients initially suffered from libido
impairment, with 10 suffering from reduced sexual potency and 6 were
infertile. Before treatment all patients suffered from low number of
erections and had a low sperm count. After 1 month of treatment
prolactin levels were significantly reduced in both groups of patients. A
notable increase in the number of erections during the first 3 months
was recorded and continued throughout the 6 months of treatment.
However the improvements in seminal fluid parameters and sexual
function were more evident and rapid in patients treated with
cabergoline. A significant increase in the serum levels of testosterone
and dihydrotestosterone were also recorded. At the beginning of
treatment, mild side-effects were recorded in 2 patients using
cabergoline compared to 5 in the bromocriptine patients.
Conclusion:
It is now recognised that the stimulation of dopamine can
enhance sexual arousal and this has been shown to occur with drugs
such as bromocriptine, deprenyl and Sinemet®. Now that prolactin is
being recognised as an inhibitor of sexual function and desire, a drug
such as cabergoline that enhances dopamine levels and reduces
prolactin levels is being heralded as a significant libido enhancer-
despite the fact that it has not yet been approved for this purpose.
Dosage:
Take 0.25mg or 0.5mg no more than twice per week, unless treating a
serious medical disorder whereupon the dosage may differ according to
your physician’s guidance, usually built up slowly to no more than 1mg
twice weekly.
Side effects:
Nausea, headache, dizziness and constipation.